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FDA 510(k)

GRINDGUARD

K-Number: K082723 · 2009-08-31

ApplicantGrind Guard Technologies, LLC
Decision Date2009-08-31
Product CodeMQC
DecisionSubstantially Equivalent

Device Summary

GRINDGUARD is the device name listed in this FDA 510(k) record. The listed applicant is Grind Guard Technologies, LLC. It received FDA 510(k) clearance on 2009-08-31 under 510(k) number K082723. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRINDGUARD?

GRINDGUARD is a medical device that received FDA 510(k) clearance on 2009-08-31. The listed applicant is Grind Guard Technologies, LLC. The 510(k) number is K082723.

When did GRINDGUARD receive FDA 510(k) clearance?

GRINDGUARD received FDA 510(k) clearance on 2009-08-31, under 510(k) number K082723.

Who is the listed applicant for GRINDGUARD?

The FDA 510(k) record lists Grind Guard Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GRINDGUARD?

The FDA product code for GRINDGUARD is MQC.

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Related Devices (Code: MQC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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